Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1864532Generated: October 30, 2026

Bromine → Ethyl 5-bromothiophene-3-carboxylate

https://huagongshe.com/reaction/1864532

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromineHCID 24408—
Reactant3-Thiophenecarboxylic acid, ethyl esterHCID 79824—
ReactantAluminum(III) ChlorideHCID 6451240—
SolventDichloromethaneHCID 6344—
ProductEthyl 5-bromothiophene-3-carboxylateHCID 1529321657.1%

Reaction Conditions

Temperature0 °C

Reaction Steps

20 g (147 mmol) of aluminum chloride are added portionwise to a solution of 10 g (67 mmol) of ethyl thiophene-3-carboxylate in 160 ml of dichloromethane, cooled beforehand to 0° C. The reaction medium is warmed to room temperature and a solution of 4 ml (73 mmol) of bromine in 10 ml of dichloromethane is then added. After reaction for 50 minutes at room temperature, the reaction medium is poured into a water+ice mixture and extracted with dichloromethane. The organic phase is dried over magnesium sulfate, filtered and evaporated under vacuum. The residue obtained is purified by chromatography on a column of silica eluted with a 9/1 heptane/ethyl acetate mixture. 9 g (57%) of ethyl 5-bromothiophene-3-carboxylate are obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07625914B2
Source datasetuspto-grants-2009_12
ORD IDord-8772cdd9810d4103844c9d7355df57b1
Source noteuspto-grants-2009_12